Canonical Allele Identifier: CA368538679

Gene: TFR2

Linked Data

• MyVariant Identifiers: chr7:g.100238836T>A (hg19) ; chr7:g.100641213T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100641213T>A , CM000669.2:g.100641213T>A	GRCh38
NC_000007.13:g.100238836T>A , CM000669.1:g.100238836T>A	GRCh37
NC_000007.12:g.100076772T>A	NCBI36
NG_007989.1:g.5338A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000223051.8:c.49A>T MANE Select	ENSP00000223051.3:p.Arg17Ter
ENST00000223051.7:c.49A>T	ENSP00000223051.3:p.Arg17Ter
ENST00000431692.5:c.49A>T	ENSP00000413905.1:p.Arg17Ter
ENST00000462107.1:c.49A>T	ENSP00000420525.1:p.Arg17Ter
ENST00000465294.5:n.54A>T
ENST00000474947.1:n.207A>T
NM_003227.3:c.49A>T	NP_003218.2:p.Arg17Ter
XM_005250553.3:c.49A>T	XP_005250610.1:p.Arg17Ter
XM_005250554.3:c.49A>T	XP_005250611.1:p.Arg17Ter
XM_005250553.4:c.49A>T	XP_005250610.1:p.Arg17Ter
XM_017012573.1:c.49A>T	XP_016868062.1:p.Arg17Ter
NM_003227.4:c.49A>T MANE Select	NP_003218.2:p.Arg17Ter